Abstract
Clefts of the lip and/or palate (CLP) are common birth defects of complex aetiology. CLP can occur in isolation or as part of a broad range of chromosomal, Mendelian or teratogenic syndromes. Although there has been marked progress in identifying genetic and environmental triggers for syndromic CLP, the aetiology of the more common non-syndromic (isolated) forms remains poorly characterized. Recently, using a combination of epidemiology, careful phenotyping, genome-wide association studies and analysis of animal models, several distinct genetic and environmental risk factors have been identified and confirmed for non-syndromic CLP. These findings have advanced our understanding of developmental biology and created new opportunities for clinical translational research. © 2011 Macmillan Publishers Limited. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 167-178 |
| Number of pages | 11 |
| Journal | Nature Reviews Genetics |
| Volume | 12 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Mar 2011 |
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